Addition Polymers

Lajoy Tucker

Teacher

Lajoy Tucker

Introduction and Definition

  • Addition polymerisation – many alkene molecules join to make one long polymer chain.

  • The C=C opens. New C–C single bonds form between units.

    Diagram showing addition polymerisation of propene monomers to form poly(propene), highlighting the repeating unit formed when the carbon–carbon double bonds open and link together in a polymer chain.

Key Terms

  • Monomer – the small repeating molecule (usually an alkene).

  • Polymer – large molecule made from many monomers.

  • Repeating unit – the smallest section of the polymer chain that repeats.

No answer provided.

How to draw the polymer (from a monomer)

1. Draw the monomer clearly around its C=C.

2. Open the double bond to two single bonds that continue out of the unit.

3. Put square brackets around the unit and add a small n outside.

Equation showing addition polymerisation of propene molecules to form poly(propene), where the carbon–carbon double bond opens to produce a repeating polymer chain

How to find the monomer (from a polymer)

1. Take one repeating unit from the chain.

2. Close the opened bonds to form a double bond.

3. Name the alkene monomer.

Diagram comparing pent-1-ene monomer with the repeating unit formed during addition polymerisation, showing the carbon–carbon double bond converted into single bonds in the polymer chain.

Exam Tips

  • For a repeating unit, draw no “n” on the unit itself.

  • Show the continuation bonds at each end of the brackets.

  • Name as poly(monomer name) – e.g. poly(propene).

  • Forgetting the continuation bonds at each bracket end.

  • Writing n next to the monomer when the question only asks for the repeating unit.

  • Misnaming: write poly(propene), not “polypropylene” unless the spec allows it.

No answer provided.

Reactivity of Addition Polymers

  • Addition polymers are unreactive due to:

    • Strong C–C and C–H bonds

    • No reactive functional groups

  • They are saturated, chemically stable, and resist biological degradation.


Intermolecular Forces in Polymers

  • Intermolecular forces determine physical properties like melting point, flexibility, and hardness.

Examples:

  • Poly(ethene): flexible, low melting point due to weak van der Waals forces.

  • Poly(chloroethene) (PVC): stronger dipole–dipole interactions due to polar C–Cl bonds. Waterproof.


Use of PVC and Modification with Plasticisers

  • PVC (poly(chloroethene)) is naturally rigid due to strong intermolecular forces between chains.

  • Addition of plasticisers:

    • Weakens intermolecular forces

    • Increases flexibility

    • Allows PVC to be used in applications like cable insulation, flooring, and clothing.

Practice Question

Example 1

Draw the repeating unit of the polymer formed from propene.

Answer:

-[–CH₂–CH(CH₃)–]-ₙ

(Ensure square brackets and extension bonds are drawn.)

Example 2

Name the monomer used to form poly(phenylethene).

Answer:

Phenylethene

Example 3

The structure of a polymer is shown. Deduce the structure of the monomer.

-[–CH₂–CHBr–]-ₙ

Answer:

CH₂=CHBr (bromoethene)